Archives: Resources
Quality Control
International Clinical Trials article discussing a rigorous protocol risk assessment method to design customized, adaptive monitoring plans.
The Patient as the Collaborator
PPD® Consulting offers insights on orphan drugs.
Flow Cytometry
Contract Pharma article about how PPD employs flow cytometry in its development of biomarker assays for client studies.
New Growth and Decline in Asia Clinical Trials
Clinical trial demands are high for the growing expertise in Asian countries.
The Dynamic Evolution of Multi-sponsor REMS
A brief background of REMS programs; dramatic shifts in the types of REMS approved; challenges associated with multi-sponsor REMS; and how to ensure that your company and products are prepared.
Adapting to Adaptive Drug Development
Jürgen Hummel, PPD’s associate statistical science director, was featured in the June issue of PharmaVOICE.
Innovation Tied to Globalization & Collaboration
The article discusses the increasing frequency and value of strategic partnerships in driving research advancements.
Better Development of Biosimilars
In the May/June 2013 issue of Drug Discovery & Development, PPD experts discuss how Bayesian modeling can leverage data to aid development of biosimilars.
Biosimilars Update Contract Pharma
PPD’s Dirk Reitsma VP and therapeutic head for oncology, was a featured subject matter expert in the April issue of Contract Pharma.